Literature DB >> 434891

Familial occurrence of omphalocele suggesting sex-linked inheritance.

S Havalad, H Noblett, B D Speidel.   

Abstract

A family is described in which 4 males in two generations had omphalocele. There was no case of omphalocele in any of the women. It is suggested that the mode of inheritance could be a sex-linked recessive trait.

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Year:  1979        PMID： 434891      PMCID： PMC1545351          DOI： 10.1136/adc.54.2.142

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  4 in total

1.  An investigation of 69 cases of exomphalos.

Authors:  T MCKEOWN; B MACMAHON; R G RECORD
Journal:  Am J Hum Genet       Date:  1953-06       Impact factor: 11.025

2.  Four cases of omphalocele in two generations of the same family.

Authors:  A Osuna; S Lindham
Journal:  Clin Genet       Date:  1976-03       Impact factor: 4.438

3.  Familial occurrence of omphalocele.

Authors:  H D Rott; H Truckenbrodt
Journal:  Humangenetik       Date:  1974

4.  Exomphalos with macroglossia: a study of eleven cases.

Authors:  I M Irving
Journal:  J Pediatr Surg       Date:  1967-12       Impact factor: 2.545
  4 in total
  3 in total

1.  Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.

Authors:  Uppala Radhakrishna; Swapan K Nath; Ken McElreavey; Uppala Ratnamala; Celi Sun; Amit K Maiti; Maryline Gagnebin; Frédérique Béna; Heather L Newkirk; Andrew J Sharp; David B Everman; Jeffrey C Murray; Charles E Schwartz; Stylianos E Antonarakis; Merlin G Butler
Journal:  J Med Genet       Date:  2012-04       Impact factor: 6.318

2.  Etiological study of omphalocele.

Authors:  A Czeizel; M Vitéz
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Familial omphalocele.

Authors:  K Steele; N C Nevin
Journal:  Ulster Med J       Date:  1985-10
  3 in total

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